Accuracy of Guided Implant Placement Using Double Versus Triple Scan Protocol in Completely Edentulous Patients

November 5, 2017 updated by: Mostafa mohamed el maghraby, Cairo University

Accuracy of Guided Implant Placement Using Double Versus Triple Scan Protocol in Completely Edentulous Patients : Randomized Clinical Trial

16 implant placement by surgical guide using double scan protocol versus triple scan protocol to Evaluate angular and linear deviation of virtual implants and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

In this study we discuss linear and angular deviation of actual implant position using planning protocol C1(double scan technique) or C2 (triple scan technique) in completely edentulous patient .

Both protocols C1(double scan technique) and C2 (triple scan technique) indicated in completely edentulous patient and require C.T scan for patient wearing scan appliance .

In C1(double scan technique) , after CT scan for patient wearing scan appliance , two optical scan for the model with and without scan appliance.

In C2 (triple scan technique) , after CT scan for patient wearing scan appliance , CT scan for scan appliance alone .

Teeth positions in both protocols were identified by radio-opaque scan appliance .

16 implant placement by surgical guide using double scan protocol versus triple scan protocol ( two groups - 8 implants in each group ) to Evaluate angular and linear deviation of virtual implants and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .

Study Type

Observational

Enrollment (Anticipated)

16

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

patients receiving dental implants in both arches by guided surgery using double versus triple scan protocol .

Description

Inclusion Criteria:

  1. patients totally edentulous arches.
  2. patients with Bucco-lingual bone thickness >6 mm allowing flapless implant placement
  3. patients free from any systemic diseases that may affect bone quality e.g diabetes.

Exclusion Criteria:

  1. patients with thin ridges.
  2. patients with systemic disease that may affect bone quality.
  3. Patients with poor oral hygiene and active periodontal diseases.
  4. Anatomical situations requiring regenerative procedure.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
double scan protocol
In C1(double scan technique) , after CT scan for patient wearing scan appliance , two optical scan for the model with and without scan appliance.
triple scan protocol
In C2 (triple scan technique) , after CT scan for patient wearing scan appliance , CT scan for scan appliance alone .
Scanning strategy is based on multiple scans. Essentially one CT scan of the patient (usually with a scan appliance). Another CT scan of the model or scan appliance may be required (double scan technique). Such a second CT scan can be replaced by optical scanning of the model and scan appliance (triple scan technique).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of angular deviation between planned implants in surgical guide and actual implant position in completely edentulous patients .
Time Frame: immediate post operative
Evaluation of angular deviation between planned implants in surgical guide and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .
immediate post operative

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of linear deviation between planned implants in surgical guide and actual implant position in completely edentulous patients
Time Frame: immediate post operative
Evaluation of linear deviation between planned implants in surgical guide and actual implant position in completely edentulous patients according to scanning protocol C1(double scan technique) and C2 (triple scan technique) .
immediate post operative

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

November 20, 2017

Primary Completion (Anticipated)

February 1, 2018

Study Completion (Anticipated)

February 1, 2018

Study Registration Dates

First Submitted

October 22, 2017

First Submitted That Met QC Criteria

October 24, 2017

First Posted (Actual)

October 25, 2017

Study Record Updates

Last Update Posted (Actual)

November 7, 2017

Last Update Submitted That Met QC Criteria

November 5, 2017

Last Verified

November 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • Cebc.cu. cairo university

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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